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Contiennent :
Aiguille de tuohy à double orifice : un pour l’émergence de l’aiguille spinale et un pour la mise en place du cathéter
Seringue de repérage Perifix® LOR
Filtre Perifix® avec système de fixation PinPad
Raccord de connexion pour cathéter Perifix®
Cathéter Perifix® Standard ou Soft Tip
Aiguille spinale Spinocan® ou Pencan®
Docking-System en option : écrou conçu pour bloquer l’avancée de l’aiguille spinale
Destination : dispositifs pour procédures de péri-rachianesthésie combinée avec connecteur NRFit®, conformes à la norme ISO 80369-6
Dispositifs médicaux de classe III. Certificat CE délivré par TÜV SUD (CE 0123)
Fabriqués par B. Braun Melsungen AG (Allemagne)
Riques résiduels/effets secondaires : Hypotension, hypothermie, arrêt cardiaque, complications neurologiques temporaires ou permanentes. Pour les autres risques résiduels, consulter la notice.
Produits non pris en charge au titre de la Liste des Produits et Prestations Remboursables
Lire attentivement les instructions figurant dans la notice et/ou sur l'étiquetage
Edition 04/2025
AST_20250109
